Inhibition of experimental diabetic cataract by topical administration of RS-verapamil hydrochloride
Aim: To investigate the efficacy of verapamil eye drops for inhibition of diabetic cataract in rats. Methods: Diabetes was induced in 69 male Sprague-Dawley rats by an intraperitoneal injection of streptozotocin (65 mg/kg body weight). One group (DV) of animals was treated by instillation of one dro...
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Published in: | British journal of ophthalmology Vol. 88; no. 1; pp. 44 - 47 |
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Abstract | Aim: To investigate the efficacy of verapamil eye drops for inhibition of diabetic cataract in rats. Methods: Diabetes was induced in 69 male Sprague-Dawley rats by an intraperitoneal injection of streptozotocin (65 mg/kg body weight). One group (DV) of animals was treated by instillation of one drop of 0.2% RS-verapamil hydrochloride in both eyes three times daily for 8 weeks. The placebo treated group (D) received the vehicle solution only. After 8 weeks the lenses were removed, inspected, and photographed using bright and dark field illumination. The transmission of He-Ne laser light was measured in the optical axis of each lens in order to determine the turbidity coefficient (t) as a measure of central lens opacity. Following digital image analysis, the integrated density as a measure of central and mid-peripheral opacities was determined. Results: Lenses of both groups developed peripheral cortical opacities not affecting the optical axis. Advanced and paracentral cortical opacities were present in 10 (16.7%) of the placebo treated lenses (D) and two (3.8%) of the verapamil treated lenses (DV). Complete corticonuclear cataract developed in four (6.7%) of the lenses from group D but none of the lenses from group DV. The mean lens turbidity t was determined to be 0.019 (SEM 0.002) mm−1 (n = 52) in the verapamil treated diabetic rats (DV) and 0.042 (0.008) mm−1 (n = 60) in the placebo treated group (D). This difference was statistically significant (p = 0.0054). The mean integrated density was 274.91 (22.5) in group D (n = 60) and 196.28 (20.7) in group DV (n = 37). This difference was also significant (p = 0.0037). Conclusion: Verapamil eye drops 0.2% administered three times daily are effective in inhibiting the progression of lens opacities in streptozotocin diabetic rats. |
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AbstractList | To investigate the efficacy of verapamil eye drops for inhibition of diabetic cataract in rats.
Diabetes was induced in 69 male Sprague-Dawley rats by an intraperitoneal injection of streptozotocin (65 mg/kg body weight). One group (DV) of animals was treated by instillation of one drop of 0.2% RS-verapamil hydrochloride in both eyes three times daily for 8 weeks. The placebo treated group (D) received the vehicle solution only. After 8 weeks the lenses were removed, inspected, and photographed using bright and dark field illumination. The transmission of He-Ne laser light was measured in the optical axis of each lens in order to determine the turbidity coefficient (t) as a measure of central lens opacity. Following digital image analysis, the integrated density as a measure of central and mid-peripheral opacities was determined.
Lenses of both groups developed peripheral cortical opacities not affecting the optical axis. Advanced and paracentral cortical opacities were present in 10 (16.7%) of the placebo treated lenses (D) and two (3.8%) of the verapamil treated lenses (DV). Complete corticonuclear cataract developed in four (6.7%) of the lenses from group D but none of the lenses from group DV. The mean lens turbidity t was determined to be 0.019 (SEM 0.002) mm(-1) (n = 52) in the verapamil treated diabetic rats (DV) and 0.042 (0.008) mm(-1) (n = 60) in the placebo treated group (D). This difference was statistically significant (p = 0.0054). The mean integrated density was 274.91 (22.5) in group D (n = 60) and 196.28 (20.7) in group DV (n = 37). This difference was also significant (p = 0.0037).
Verapamil eye drops 0.2% administered three times daily are effective in inhibiting the progression of lens opacities in streptozotocin diabetic rats. Aim: To investigate the efficacy of verapamil eye drops for inhibition of diabetic cataract in rats. Methods: Diabetes was induced in 69 male Sprague-Dawley rats by an intraperitoneal injection of streptozotocin (65 mg/kg body weight). One group (DV) of animals was treated by instillation of one drop of 0.2% RS-verapamil hydrochloride in both eyes three times daily for 8 weeks. The placebo treated group (D) received the vehicle solution only. After 8 weeks the lenses were removed, inspected, and photographed using bright and dark field illumination. The transmission of He-Ne laser light was measured in the optical axis of each lens in order to determine the turbidity coefficient (t) as a measure of central lens opacity. Following digital image analysis, the integrated density as a measure of central and mid-peripheral opacities was determined. Results: Lenses of both groups developed peripheral cortical opacities not affecting the optical axis. Advanced and paracentral cortical opacities were present in 10 (16.7%) of the placebo treated lenses (D) and two (3.8%) of the verapamil treated lenses (DV). Complete corticonuclear cataract developed in four (6.7%) of the lenses from group D but none of the lenses from group DV. The mean lens turbidity t was determined to be 0.019 (SEM 0.002) mm−1 (n = 52) in the verapamil treated diabetic rats (DV) and 0.042 (0.008) mm−1 (n = 60) in the placebo treated group (D). This difference was statistically significant (p = 0.0054). The mean integrated density was 274.91 (22.5) in group D (n = 60) and 196.28 (20.7) in group DV (n = 37). This difference was also significant (p = 0.0037). Conclusion: Verapamil eye drops 0.2% administered three times daily are effective in inhibiting the progression of lens opacities in streptozotocin diabetic rats. Aim: To investigate the efficacy of verapamil eye drops for inhibition of diabetic cataract in rats. Methods: Diabetes was induced in 69 male Sprague-Dawley rats by an intraperitoneal injection of streptozotocin (65 mg/kg body weight). One group (DV) of animals was treated by instillation of one drop of 0.2% RS-verapamil hydrochloride in both eyes three times daily for 8 weeks. The placebo treated group (D) received the vehicle solution only. After 8 weeks the lenses were removed, inspected, and photographed using bright and dark field illumination. The transmission of He-Ne laser light was measured in the optical axis of each lens in order to determine the turbidity coefficient (t) as a measure of central lens opacity. Following digital image analysis, the integrated density as a measure of central and mid-peripheral opacities was determined. Results: Lenses of both groups developed peripheral cortical opacities not affecting the optical axis. Advanced and paracentral cortical opacities were present in 10 (16.7%) of the placebo treated lenses (D) and two (3.8%) of the verapamil treated lenses (DV). Complete corticonuclear cataract developed in four (6.7%) of the lenses from group D but none of the lenses from group DV. The mean lens turbidity t was determined to be 0.019 (SEM 0.002) mm -1 (n = 52) in the verapamil treated diabetic rats (DV) and 0.042 (0.008) mm-1 (n = 60) in the placebo treated group (D). This difference was statistically significant (p = 0.0054). The mean integrated density was 274.91 (22.5) in group D (n = 60) and 196.28 (20.7) in group DV (n = 37). This difference was also significant (p = 0.0037). Conclusion: Verapamil eye drops 0.2% administered three times daily are effective in inhibiting the progression of lens opacities in streptozotocin diabetic rats. AIMTo investigate the efficacy of verapamil eye drops for inhibition of diabetic cataract in rats.METHODSDiabetes was induced in 69 male Sprague-Dawley rats by an intraperitoneal injection of streptozotocin (65 mg/kg body weight). One group (DV) of animals was treated by instillation of one drop of 0.2% RS-verapamil hydrochloride in both eyes three times daily for 8 weeks. The placebo treated group (D) received the vehicle solution only. After 8 weeks the lenses were removed, inspected, and photographed using bright and dark field illumination. The transmission of He-Ne laser light was measured in the optical axis of each lens in order to determine the turbidity coefficient (t) as a measure of central lens opacity. Following digital image analysis, the integrated density as a measure of central and mid-peripheral opacities was determined.RESULTSLenses of both groups developed peripheral cortical opacities not affecting the optical axis. Advanced and paracentral cortical opacities were present in 10 (16.7%) of the placebo treated lenses (D) and two (3.8%) of the verapamil treated lenses (DV). Complete corticonuclear cataract developed in four (6.7%) of the lenses from group D but none of the lenses from group DV. The mean lens turbidity t was determined to be 0.019 (SEM 0.002) mm(-1) (n = 52) in the verapamil treated diabetic rats (DV) and 0.042 (0.008) mm(-1) (n = 60) in the placebo treated group (D). This difference was statistically significant (p = 0.0054). The mean integrated density was 274.91 (22.5) in group D (n = 60) and 196.28 (20.7) in group DV (n = 37). This difference was also significant (p = 0.0037).CONCLUSIONVerapamil eye drops 0.2% administered three times daily are effective in inhibiting the progression of lens opacities in streptozotocin diabetic rats. Aim: To investigate the efficacy of verapamil eye drops for inhibition of diabetic cataract in rats. Methods: Diabetes was induced in 69 male Sprague-Dawley rats by an intraperitoneal injection of streptozotocin (65 mg/kg body weight). One group (DV) of animals was treated by instillation of one drop of 0.2% RS-verapamil hydrochloride in both eyes three times daily for 8 weeks. The placebo treated group (D) received the vehicle solution only. After 8 weeks the lenses were removed, inspected, and photographed using bright and dark field illumination. The transmission of He-Ne laser light was measured in the optical axis of each lens in order to determine the turbidity coefficient (t) as a measure of central lens opacity. Following digital image analysis, the integrated density as a measure of central and mid-peripheral opacities was determined. Results: Lenses of both groups developed peripheral cortical opacities not affecting the optical axis. Advanced and paracentral cortical opacities were present in 10 (16.7%) of the placebo treated lenses (D) and two (3.8%) of the verapamil treated lenses (DV). Complete corticonuclear cataract developed in four (6.7%) of the lenses from group D but none of the lenses from group DV. The mean lens turbidity t was determined to be 0.019 (SEM 0.002) mm −1 (n = 52) in the verapamil treated diabetic rats (DV) and 0.042 (0.008) mm −1 (n = 60) in the placebo treated group (D). This difference was statistically significant (p = 0.0054). The mean integrated density was 274.91 (22.5) in group D (n = 60) and 196.28 (20.7) in group DV (n = 37). This difference was also significant (p = 0.0037). Conclusion: Verapamil eye drops 0.2% administered three times daily are effective in inhibiting the progression of lens opacities in streptozotocin diabetic rats. |
Audience | Professional Academic |
Author | Daxer, A Ettl, A Göttinger, W Schmid, E |
AuthorAffiliation | 1 Department of Ophthalmology, University of Innsbruck, Austria 3 Eye Center, Linz, Austria 2 Department of Neuro-Ophthalmology, Oculoplastic and Orbital Surgery, Central Hospital, Pölten, Austria |
AuthorAffiliation_xml | – name: 1 Department of Ophthalmology, University of Innsbruck, Austria – name: 3 Eye Center, Linz, Austria – name: 2 Department of Neuro-Ophthalmology, Oculoplastic and Orbital Surgery, Central Hospital, Pölten, Austria |
Author_xml | – sequence: 1 givenname: A surname: Ettl fullname: Ettl, A organization: Eye Center, Linz, Austria – sequence: 2 givenname: A surname: Daxer fullname: Daxer, A organization: Eye Center, Linz, Austria – sequence: 3 givenname: W surname: Göttinger fullname: Göttinger, W organization: Eye Center, Linz, Austria – sequence: 4 givenname: E surname: Schmid fullname: Schmid, E organization: Eye Center, Linz, Austria |
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Keywords | Endocrinopathy Human Cataract Chemoprophylaxis Diabetes mellitus Calcium antagonist Prevention Eye disease Lens disease Aralkylamine Verapamil Anterior segment disease Topical administration |
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Notes | Correspondence to: Armin Ettl, MD, PhD Neuro-Ophthalmology, Zentraltrankenhaus Postfach 176, A-3100 St Pölten, Austria; a.ettl@kh-st-poelten.at href:bjophthalmol-88-44.pdf local:0880044 ark:/67375/NVC-6P9K7G9S-H istex:3C6188DC6C98028E931197173786ECC1A594841D PMID:14693771 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Preliminary results of this study were presented at the annual meetings of the AER in Granada in 1993 and the ARVO in Fort Lauderdale in 1995. Correspondence to: Armin Ettl, MD, PhD Neuro-Ophthalmology, Zentraltrankenhaus Postfach 176, A-3100 St Pölten, Austria; a.ettl@kh-st-poelten.at |
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Snippet | Aim: To investigate the efficacy of verapamil eye drops for inhibition of diabetic cataract in rats. Methods: Diabetes was induced in 69 male Sprague-Dawley... To investigate the efficacy of verapamil eye drops for inhibition of diabetic cataract in rats. Diabetes was induced in 69 male Sprague-Dawley rats by an... AIMTo investigate the efficacy of verapamil eye drops for inhibition of diabetic cataract in rats.METHODSDiabetes was induced in 69 male Sprague-Dawley rats by... Aim: To investigate the efficacy of verapamil eye drops for inhibition of diabetic cataract in rats. Methods: Diabetes was induced in 69 male Sprague-Dawley... |
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SubjectTerms | Animals Associated diseases and complications Biological and medical sciences Calcium Channel Blockers - therapeutic use Care and treatment Cataract Cataract - etiology Cataract - prevention & control Clinical Science - Scientific Reports diabetes Diabetes Mellitus, Experimental - complications Diabetes. Impaired glucose tolerance Disease Progression Endocrine pancreas. Apud cells (diseases) Endocrinopathies Image Processing, Computer-Assisted - methods Lens diseases Male Medical sciences Ophthalmic Solutions Ophthalmology Rats Rats, Sprague-Dawley verapamil Verapamil - therapeutic use |
Title | Inhibition of experimental diabetic cataract by topical administration of RS-verapamil hydrochloride |
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